Identity
- Trade Name
- Syneture FDA UDI
- Generic Name
- Suture kit, medicated FDA UDI
- Device Name
- Custom Suture Pack,(1) 88861917-61;(2) 88862615-53;(2) 88863185-51;(1) 88863186-21;(4) 88863205-61;(1) 88863256-51;(2) CL-803;(1) SC-691;(1) VP-331-X;(1) VP-522-X;(1) VP-902-X FDA UDI
- Model / Reference
- US1679 FDA UDI
- Description
- Custom Suture Pack,(1) 88861917-61;(2) 88862615-53;(2) 88863185-51;(1) 88863186-21;(4) 88863205-61;(1) 88863256-51;(2) CL-803;(1) SC-691;(1) VP-331-X;(1) VP-522-X;(1) VP-902-X FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521211988 FDA UDI
- FDA Product Code
- OVN FDA UDI
- GMDN Term
- Suture kit, medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4830 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Syneture by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Covidien LP
Sources (1)
- FDA UDI 0ee5bcc1-dc1a-4852-9516-2ae13e1dc714 36 fields · synced Jun 6, 2026